A AND D PLUS E- petrolatum ointment

A and D plus E by

Drug Labeling and Warnings

A and D plus E by is a Otc medication manufactured, distributed, or labeled by H&H Laboratories, Inc., H&H Laboratories, Inc. . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient (in each gram): White Petrolatum 93.5%

PURPOSE

Purpose-Skin Protectant

INDICATIONS & USAGE

Uses-Temporarily protects minor cuts, scrapes, and sunburn.     Helps treat and prevent diaper rash.  Protects chafed skin or minor skin irritation associated with diaper rash and helps seal out wetness. Temporarily protects and helps chapped or cracked skin and lips.  Helps protect lips from drying effects of wind and cold weather.

DOSAGE & ADMINISTRATION

Directions: Apply liberally as needed  Change wet and soiled diapers promptly.  Cleanse the diaper area and allow to dry. Use with each diaper change, especially at bedtime when exposure to wet diapers may be prolonged.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

WARNINGS

For external use only.  Do not use in eyes, on deep puncture wounds, animal bites, or serious burns or for more than 1 week unless directed by a doctor.

Stop use and ask a doctor if: A rash or allergic reaction develops.  Condition worsens, persists, or recurs.

INACTIVE INGREDIENT

Inactive Ingredients: Corn Oil, Light Mineral Oil, Vitamin A Palmitate, Vitamin D, Vitamin E

PRINCIPAL DISPLAY PANEL

MM1

MM2

INGREDIENTS AND APPEARANCE

A AND D PLUS E 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52471-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	937.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ERGOCALCIFEROL (UNII: VS041H42XC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52471-100-04	113 g in 1 TUBE
2	NDC: 52471-100-13	168 g in 1 JAR
3	NDC: 52471-100-16	454 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	05/14/2012

Labeler - H&H Laboratories, Inc. (151357175)

Registrant - H&H Laboratories, Inc. (151357175)